CTRI/2023/06/053848招募中4 期
Adverse drug reactions in multi-drug resistant pulmonary tuberculosis patients receiving Bedaquiline containing shorter oral regimen: Post marketing surveillance & assessment
试验速览
- 阶段
- 4 期
- 状态
- 招募中
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Observational
入排标准
入选标准
- •1)Patients above the age of 18 years
- •2)Patients diagnosed with Multidrug resistant pulmonary tuberculosis (Rifampicin resistance detected/inferred; MDR-TB with H resistance detected/inferred based on InhA mutation only or based on KatG mutation only (not both); MDR-TB with FQ resistance not detected)
- •3)Those who will understand the purpose of the study, ready to provide information regarding their health status and written informed consent for participation in the study.
排除标准
- •1)Pregnant and lactating women
- •2)History of exposure for more than 1 month to Bedaquiline, Levofloxacin, Ethionamide or Clofazimine
- •3)Patients with H resistance detected with both KatG and InhA mutation; and patients with FQ resistance detected
- •4)Confirmed resistance to a medicine in the shorter oral Bedaquiline- containing MDR-TB regimen
- •5)History of Torsade de Pointes, congenital long QT syndrome, uncompensated heart failure, and cardio ventricular arrythmias
- •6)Intolerance to any drug in the regimen or risk of toxicity from a drug in shorter oral Bedaquiline- containing MDR-TB regimen
- •7)Extra-pulmonary TB disease
- •8)Extensive TB disease found in presence of bilateral cavitary disease or extensive parenchymal damage on chest radiography
- •9)Reactive Serology for HIV
研究者
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